Allele Registry

Canonical Allele Identifier: PA2827515251

Gene: TOP3B HGNC NCBI

ClinVar RCV:

RCV004180510

ClinVar Variation:

2338671

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336777.1:p.Val628Met	CA410834571 NM_001349848.2:c.1882G>A